NCT03133286

Radiotherapy Assessments During Intervention ANd Treatment (RADIANT)

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 16 (actual)
• Sponsor: DxTerity Diagnostics · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Collect blood samples and associated clinical data prior to, during, and post radiation treatment.

Detailed description

In order to further refine and independently validate the performance of DxTerity's test developed during the previous pilot study, the study will collect pre-, during, and post-irradiation blood samples and associated clinical and self-reported information from up to five hundred (500) subjects for analysis. Patients with a diagnosis of primary gastrointestinal (GI), genitourinary (GU), or gynecological (GYN) cancer requiring radiation treatment to the primary disease site will be included in the study. Combining chemotherapy is allowed. Blood samples for this study will be collected from cancer patients scheduled to undergo radiation therapy prior to and either during or after treatment. Approximately 150μL of blood per time point will be obtained via fingerstick remotely, from the participant's home or doctor's office; participation in this study will not affect any aspect of patient treatment. Samples will be collected using DxTerity's proprietary DxCollect® MCD Fingerstick Kit (MCD).

Conditions

• Radiation Therapy
• Cancer
• Cancer of Anus
• Cancer of Bladder
• Cancer of Cervix
• Cancer of Colon
• Cancer of Rectum
• Cancer of Esophagus
• Cancer of Gallbladder
• Cancer of Liver
• Cancer of Ovary
• Cancer of Pancreas
• Cancer of Prostate
• Cancer of Kidney and Renal Pelvis
• Cancer of Stomach
• Cancer of Testis
• Cancer of Uterus
• Cancer of Uterus and Cervix
• Cancer of Kidney

Timeline

• Start date: 2017-04-06
• Primary completion: 2020-02-24
• Completion: 2020-02-25
• First posted: 2017-04-28
• Last updated: 2024-08-07

Locations

4 sites across 1 country: United States